ABSTRACT: The co-effects of triclosan and polyvinyl chloride microplastics on partial denitrification sequencing batch reactors with different carbon source
Project description:The co-effects of triclosan and polyvinyl chloride microplastics on partial denitrification sequencing batch reactors with different carbon source
| PRJNA730365 | ENA
Project description:Response of bacterial community to original and aged polyvinyl chloride microplastics in sequencing batch reactors
| PRJNA1199229 | ENA
Project description:Chronic responses of aerobic granules to polyvinyl chloride microplastics in a sequencing batch reactor performing simultaneous carbon, nitrogen and phosphorus removal
Project description:In this study, the effects of Triclosan (TCS) and its alternatives, including Benzalkonium chloride (BAM), Benzethonium chloride (BEC), Chloroxylenol (CEO), Chlorhexidine (CHX) and Cetylpyridinium chloride (CPC), were investigated in THP-1 macrophages. For this purpose, untargeted proteomics was applied.
2024-02-05 | PXD044828 | Pride
Project description:Effects of polyvinyl chloride microplastics and benzylalkyldimethylethyl compounds on system performance, microbial community and resistance genes in sulfur autotrophic denitrification system
| PRJNA1071514 | ENA
Project description:Effect of triclosan on partial denitrification, microbial community and antibiotic resistance genes (ARGs) of a sequencing biofilm batch reactor (SBBR)
Project description:The influence of different nitrogen sources on transcriptome of Purple non sulfur bacterium R. Capsulatus was investigated by comparing expression profile on 5mM ammonium chloride and 2 mM glutamate. Carbon source was 40mM acetate on both conditions. To study the effect of different acetate concentrations, 40mM and 80mM acetate were used with 2 mM glutamate as nitrogen source.
Project description:Caldicellulosiruptor bescii is an anaerobic hyper thermophile that can utilize a wide range of substrates. However, inhibitors released from biomass can result in unfavorable growth conditions and limit bioconversion to products. Medium as well as intracellular pH are conditions critical for growth and prone to change in effect of fermentation end or by products such as, CO2, organic acids etc. Growth pH for C. bescii as currently reported is a narrow range of 6.8-7.3. In this study, we examined the physiological and systems level responses of C. bescii to growth at acidic pH. Samples collected from bottles, controlled batch, fed-batch and chemostat systems were subjected to growth, product and integrated omics profiling. It was discovered that in batch reactors, lowering pH from 7.2 to 6.0 at the mid-log phase, led to a significant increase in growth and product yields. Time course transcriptomics data collected from these batch reactors was analyzed to try and get a better understanding of the underlying mechanisms for improved growth.
